Fibrodysplasia Ossificans Progressiva

Known as: Progressive myositis ossificans, MUENCHMEYER SYNDROME, Progressive Ossifying Myositis 
A condition in which there is progressive heterotopic bone formation of the tendons and muscles.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1935-2018
020406019352017

Papers overview

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2015
2015
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease characterized by extraskeletal bone formation through… (More)
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Review
2015
Review
2015
Myositis ossificans is a self-limiting, benign ossifying lesion that can affect any type of soft tissue, including subcutaneous… (More)
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2012
2012
Fibrodysplasia ossificans progressiva (FOP; MIM #135100) is a debilitating genetic disorder of dysregulated cellular… (More)
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Highly Cited
2009
Highly Cited
2009
Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant human disorder of bone formation that causes developmental… (More)
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2008
2008
BACKGROUND Fibrodysplasia ossificans progressiva is a rare autosomal dominant disorder characterized by congenital malformation… (More)
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Highly Cited
2006
Highly Cited
2006
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder of skeletal malformations and progressive… (More)
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2001
2001
Fibrodysplasia ossificans progressiva (FOP) is a catastrophic genetic disorder of progressive heterotopic ossification associated… (More)
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Highly Cited
1996
Highly Cited
1996
BACKGROUND Fibrodysplasia ossificans progressiva is a heritable disorder of connective tissue characterized by congenital… (More)
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Highly Cited
1993
Highly Cited
1993
Forty-four patients who had fibrodysplasia ossificans progressiva responded by mail to a questionnaire regarding the age at the… (More)
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1982
1982
Complete ascertainment of fibrodysplasia ossificans progressiva in the United Kingdom was attempted and 44 patients were… (More)
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